A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268244



Internal ID20835284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180809194..180840700hg38UCSC Ensembl
chr5:180236194..180267700hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3831507
hg1931507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566913
Supporting Variants
Samples
Known GenesHEIH, LINC00847, MGAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268244
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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